| Primary Device ID | 00811714034362 |
| NIH Device Record Key | 9651ebc1-7141-4b93-be3f-43dcff555a9e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Awl |
| Version Model Number | 903001-0000 |
| Catalog Number | 903001-0000 |
| Company DUNS | 002745858 |
| Company Name | RESPONSIVE ORTHOPEDICS LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |